Simulation and optimization of tyre-based steam activated carbons production for gas-phase polycyclic aromatic hydrocarbons abatement

2012 ◽  
Vol 187 ◽  
pp. 123-132 ◽  
Author(s):  
A. Aranda ◽  
R. Murillo ◽  
T. García ◽  
A.M. Mastral
2020 ◽  
Vol 24 (3) ◽  
pp. 459-465
Author(s):  
O.O. Ijaola ◽  
A.Y. Sangodoyin

Determination and remediation of pollutants such as polycyclic aromatic hydrocarbons (PAHs) have not being fully regulated in Nigeria; hence  contamination of surface water by such pollutant is a major concern. This study was designed to determine the level of selected PAHs in petroleum contaminated water using spectroscopic techniques and the efficacy of activated carbons made from Bambusa vulgaris and Oxytenanthera  vabyssinaca. Bambusa vulgaris and Oxytenanthera abyssinaca were carbonized at 350OC and activated with Phosphoric acid (CBV350OC H3PO4) and Potassium chloride (COA 350OC KCl) as dehydrating agent respectively. The adsorbents were then used to remediate PAHs in petroleum contaminated water. Liquid-Liquid extraction procedures were used for extracting selected PAHs from sampled solutions. The batch experiment was performed to study the adsorption capacity of adsorbents at 5hrs contact time. Analysis of PAHs concentration for each sampling day was determined by GC-MS. Total PAHs in simulated wastewater did not show a clear trend, contrary to the expectation that there should be a progressive increase with time due to photolysis or photodecomposition of compounds or PAHs. COA 350OC KCl showed a range of 6.2-19.3% removal efficiency of each selected PAH with a total percentage efficiency of 27.7-70.8 for all days. For CBV350OC H3PO4 removal efficiency ranged from 10.26-19.30% for each selected PAH and a total efficiency of 50.8-100% for all selected PAHs for the 4 days intervals. The experimental result showed that adsorbent made from Bambusa vulgaris and Oxytenanthera abyssinaca and activated with H3PO4 and KCl as dehydrating agentrespectively can efficiently adsorb the selected PAHs in contaminated water. The study also revealed that PAHs in contaminated water increases with time due to photodecomposition, thus necessitating their treatment on time.


2013 ◽  
Vol 110 ◽  
pp. 494-500 ◽  
Author(s):  
Luis Gustavo T. dos Reis ◽  
Daniel Gallart-Mateu ◽  
Wagner F. Pacheco ◽  
Agustín Pastor ◽  
Miguel de la Guardia ◽  
...  

2019 ◽  
Vol 19 (13) ◽  
pp. 8741-8758 ◽  
Author(s):  
Atallah Elzein ◽  
Rachel E. Dunmore ◽  
Martyn W. Ward ◽  
Jacqueline F. Hamilton ◽  
Alastair C. Lewis

Abstract. Ambient particulate matter (PM) can contain a mix of different toxic species derived from a wide variety of sources. This study quantifies the diurnal variation and nocturnal abundance of 16 polycyclic aromatic hydrocarbons (PAHs), 10 oxygenated PAHs (OPAHs) and 9 nitrated PAHs (NPAHs) in ambient PM in central Beijing during winter. Target compounds were identified and quantified using gas chromatography–time-of-flight mass spectrometry (GC-Q-ToF-MS). The total concentration of PAHs varied between 18 and 297 ng m−3 over 3 h daytime filter samples and from 23 to 165 ng m−3 in 15 h night-time samples. The total concentrations of PAHs over 24 h varied between 37 and 180 ng m−3 (mean: 97±43 ng m−3). The total daytime concentrations during high particulate loading conditions for PAHs, OPAHs and NPAHs were 224, 54 and 2.3 ng m−3, respectively. The most abundant PAHs were fluoranthene (33 ng m−3), chrysene (27 ng m−3), pyrene (27 ng m−3), benzo[a]pyrene (27 ng m−3), benzo[b]fluoranthene (25 ng m−3), benzo[a]anthracene (20 ng m−3) and phenanthrene (18 ng m−3). The most abundant OPAHs were 9,10-anthraquinone (18 ng m−3), 1,8-naphthalic anhydride (14 ng m−3) and 9-fluorenone (12 ng m−3), and the three most abundant NPAHs were 9-nitroanthracene (0.84 ng m−3), 3-nitrofluoranthene (0.78 ng m−3) and 3-nitrodibenzofuran (0.45 ng m−3). ∑PAHs and ∑OPAHs showed a strong positive correlation with the gas-phase abundance of NO, CO, SO2 and HONO, indicating that PAHs and OPAHs can be associated with both local and regional emissions. Diagnostic ratios suggested emissions from traffic road and coal combustion were the predominant sources of PAHs in Beijing and also revealed the main source of NPAHs to be secondary photochemical formation rather than primary emissions. PM2.5 and NPAHs showed a strong correlation with gas-phase HONO. 9-Nitroanthracene appeared to undergo a photodegradation during the daytime and showed a strong positive correlation with ambient HONO (R=0.90, P < 0.001). The lifetime excess lung cancer risk for those species that have available toxicological data (16 PAHs, 1 OPAH and 6 NPAHs) was calculated to be in the range 10−5 to 10−3 (risk per million people ranges from 26 to 2053 cases per year).


2008 ◽  
Vol 454 (1-3) ◽  
pp. 30-35 ◽  
Author(s):  
Petar D. Todorov ◽  
Carola Koper ◽  
Joop H. van Lenthe ◽  
Leonardus W. Jenneskens

RSC Advances ◽  
2015 ◽  
Vol 5 (102) ◽  
pp. 84066-84075 ◽  
Author(s):  
Juan Dang ◽  
Xiangli Shi ◽  
Qingzhu Zhang ◽  
Jingtian Hu ◽  
Wenxing Wang

9-Chloroanthracene (9-ClAnt), an important member of the chlorinated polycyclic aromatic hydrocarbons (ClPAHs).


Author(s):  
M Kalaitzoglou ◽  
C Samara

AbstractParticulate- and gas-phase polycyclic aromatic hydrocarbons (PAHs) were determined in the mainstream smoke (MSS) of 59 manufactured cigarette brands (commercially available brands of unknown tobacco and blend type) with variable ‘tar’ yields and physical/technological characteristics. Depending on the existence/absence of filter, the ‘tar’ yield indicated on the packet, and the cigarette length and diameter, the examined cigarette brands were classified into 15 groups: non filter (NF), high (H), medium (M), light (L), super light (SL), ultra light (UL), one-tar yields (O), 100 mm long cigarettes (H-100, L-100, SL-100, UL-100, O-100), and slim cigarettes (SL-SLIM, UL-SLIM, O-SLIM). Cigarettes were smoked in a reference smoking machine equipped with glass fibre filters for collection of PAHs bound to total particulate matter (TPM), and polyurethane foam plugs (PUF) for collection of gas-phase PAHs. The relationships of gas- and particulate-phase concentrations of PAHs (ng/cig) with the contents of typical MSS components, such as TPM, ‘tar’, nicotine and carbon monoxide were investigated. In addition, the phase partitioning of PAHs in MSS was evaluated in relation to the technological characteristics of cigarettes.


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